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uSINE-PAMS:人工智能驱动的超声引导下腰椎穿刺术以提高操作准确性:一项初步研究报告

uSINE-PAMS Artificial Intelligence-Driven, Ultrasound-Guided Lumbar Puncture to Improve Procedural Accuracy: A Pilot Study Report.

作者信息

Lin Xuling, Lam Mei Lyn Carissa, Chuang Ding Fang, Yuen Joanne Yong Ern, Fu Liqing, Jun Zhi Teh Valerie, Marliya Aynul, Saffari Seyed Ehsan, Lim Christen Sheng Jie, Wong Yu-Lin, Seet Ying Hao Christopher

机构信息

Department of Neurology, National Neuroscience Institute, Singapore.

Department of Research, National Neuroscience Institute, Singapore.

出版信息

Neurol Clin Pract. 2025 Apr;15(2):e200447. doi: 10.1212/CPJ.0000000000200447. Epub 2025 Feb 25.

Abstract

BACKGROUND

Traditional lumbar punctures (LPs) often fail, leading to diagnostic delays and increased risks. Ultrasound guidance provides improved success rates but faces adoption barriers due to neuraxial-ultrasound training and implementation challenges. The Ultrasound-Guided Spinal Landmark Identification With Needle Navigation System and Position and Angular Marking System (uSINE-PAMS) were designed to address these issues: uSINE is a machine-learning software for neuraxial-ultrasound guidance; PAMS is a hardware that translates ultrasound data for accurate needle insertion.

RECENT FINDINGS

A pilot study with 10 patients showed that uSINE-PAMS-guided LP achieved an 80% first-pass success rate with no complication; the median patient age was 43 years, and the median body mass index was 24.5 kg/m. The uSINE-PAMS system showed feasibility.

IMPLICATIONS FOR PRACTICE

This pilot study showed that uSINE-PAMS-guided LP is feasible with a promising first-pass success rate at 80%. An ongoing phase 2 study (NCT05824546) of uSINE-PAMS may alter future standard of practice for LPs.

TRIAL REGISTRATION INFORMATION

This pilot study is registered under ClinicalTrials.gov (ID: NCT05824546).

摘要

背景

传统腰椎穿刺(LP)常常失败,导致诊断延迟和风险增加。超声引导可提高成功率,但由于神经轴超声培训和实施方面的挑战,其应用面临障碍。超声引导下脊柱地标识别与针导航系统及位置和角度标记系统(uSINE-PAMS)旨在解决这些问题:uSINE是一种用于神经轴超声引导的机器学习软件;PAMS是一种将超声数据转化以实现精确进针的硬件。

最新发现

一项针对10名患者的试点研究表明,uSINE-PAMS引导下的LP首次穿刺成功率达到80%,且无并发症;患者年龄中位数为43岁,体重指数中位数为24.5kg/m²。uSINE-PAMS系统显示出可行性。

对实践的启示

这项试点研究表明,uSINE-PAMS引导下的LP是可行的,首次穿刺成功率有望达到80%。正在进行的uSINE-PAMS 2期研究(NCT05824546)可能会改变未来LP的实践标准。

试验注册信息

这项试点研究已在ClinicalTrials.gov(ID:NCT05824546)注册。

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